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. 2004 Feb 23;14(4):953-7.
doi: 10.1016/j.bmcl.2003.12.002.

Discovery and in vitro evaluation of potent TrkA kinase inhibitors: oxindole and aza-oxindoles

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Discovery and in vitro evaluation of potent TrkA kinase inhibitors: oxindole and aza-oxindoles

Edgar R Wood et al. Bioorg Med Chem Lett. .

Abstract

The discovery, synthesis, potential binding mode, and in vitro kinase profile of 3-(3-bromo-4-hydroxy-5-(2'-methoxyphenyl)-benzylidene)-5-bromo-1,3-dihydro-pyrrolo[2,3-b]pyridin-2-one, 3-[(1-methyl-1H-indol-3-yl)methylene]-1,3-dihydro-2H-pyrrolo[3,2-b]-pyridin-2-one as potent TrkA inhibitors are discussed.

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